Canonical Allele Identifier: CA2731107123
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2802273
ClinVar RCV Id: RCV003655615
dbSNP Id: rs2140673563
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66484974T>A , CM000677.2:g.66484974T>A GRCh38
NC_000015.9:g.66777312T>A , CM000677.1:g.66777312T>A GRCh37
NC_000015.8:g.64564366T>A NCBI36
NG_008305.1:g.103102T>A , LRG_725:g.103102T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2254T>A ENSP00000508681.1:n.628-2254T>A
ENST00000685172.1:c.694-16T>A ENSP00000509604.1:n.694-16T>A
ENST00000685763.1:c.547-16T>A ENSP00000509016.1:n.547-16T>A
ENST00000686347.1:c.569-2254T>A ENSP00000509027.1:n.569-2254T>A
ENST00000687191.1:n.1052-16T>A
ENST00000687481.1:n.93T>A
ENST00000689951.1:c.745-16T>A ENSP00000509308.1:n.745-16T>A
ENST00000691077.1:c.694-20T>A ENSP00000509843.1:n.694-20T>A
ENST00000691576.1:c.569-20T>A ENSP00000510066.1:n.569-20T>A
ENST00000691937.1:c.694-16T>A ENSP00000508768.1:n.694-16T>A
ENST00000692487.1:c.694-20T>A ENSP00000509534.1:n.694-20T>A
ENST00000692683.1:c.628-16T>A ENSP00000508437.1:n.628-16T>A
ENST00000693150.1:c.550-16T>A ENSP00000510309.1:n.550-16T>A
ENST00000307102.10:c.694-16T>A MANE Select ENSP00000302486.5:n.694-16T>A
ENST00000307102.9:c.694-16T>A ENSP00000302486.4:n.694-16T>A
ENST00000566326.1:c.166-16T>A ENSP00000456438.1:n.166-16T>A
NM_002755.3:c.694-16T>A , LRG_725t1:c.694-16T>A NP_002746.1:n.694-16T>A
XM_011521783.1:c.628-16T>A XP_011520085.1:n.628-16T>A
XM_011521783.3:c.628-16T>A XP_011520085.1:n.628-16T>A
XM_017022411.2:c.616-16T>A XP_016877900.1:n.616-16T>A
XM_017022412.1:c.550-16T>A XP_016877901.1:n.550-16T>A
XM_017022413.1:c.166-16T>A XP_016877902.1:n.166-16T>A
NM_002755.4:c.694-16T>A MANE Select NP_002746.1:n.694-16T>A
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